Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCTCCACTCACCTGGTACTGCATG[A/G]CCTGCTTCCCGACATCCATGTCCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 611616 | ||||||||||||||||||||
Literature Links: |
NADK PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NADK - NAD kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198993.1 | 756 | Missense Mutation | GCC,GTC | A,V 277 | NP_001185922.1 | |
NM_001198994.1 | 756 | Missense Mutation | GCC,GTC | A,V 422 | NP_001185923.1 | |
NM_001198995.1 | 756 | Missense Mutation | GCC,GTC | A,V 245 | NP_001185924.1 | |
NM_023018.4 | 756 | Missense Mutation | GCC,GTC | A,V 277 | NP_075394.3 | |
XM_005244778.2 | 756 | Missense Mutation | GCC,GTC | A,V 277 | XP_005244835.1 | |
XM_006710837.2 | 756 | Missense Mutation | GCC,GTC | A,V 277 | XP_006710900.1 | |
XM_006710838.2 | 756 | Missense Mutation | GCC,GTC | A,V 190 | XP_006710901.1 | |
XM_006710839.1 | 756 | Missense Mutation | GCC,GTC | A,V 381 | XP_006710902.1 | |
XM_011542006.1 | 756 | Missense Mutation | GCC,GTC | A,V 174 | XP_011540308.1 | |
XM_011542007.1 | 756 | Missense Mutation | GCC,GTC | A,V 174 | XP_011540309.1 | |
XM_011542008.1 | 756 | Missense Mutation | GCC,GTC | A,V 174 | XP_011540310.1 | |
XM_011542009.2 | 756 | Missense Mutation | GCC,GTC | A,V 174 | XP_011540311.1 | |
XM_017002143.1 | 756 | Missense Mutation | GCC,GTC | A,V 277 | XP_016857632.1 | |
XM_017002144.1 | 756 | Missense Mutation | GCC,GTC | A,V 165 | XP_016857633.1 | |
XM_017002145.1 | 756 | Missense Mutation | GCC,GTC | A,V 155 | XP_016857634.1 | |
XM_017002146.1 | 756 | Missense Mutation | GCC,GTC | A,V 155 | XP_016857635.1 |
SLC35E2 - solute carrier family 35 member E2 | ||||||
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There are no transcripts associated with this gene. |